SP50834 AND nstd71 - dbVar - NCBI

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv888986	copy number variation	1	nstd71	human		NCBI36 chr7: 110,670,566-111,138,748 , GRCh37.p13 chr7: 110,883,330-111,351,512 , GRCh38.p12 chr7: 111,243,274-111,711,456	LOC100420226, IMMP2L
nsv890803	copy number variation	10	nstd71	human		NCBI36 chr8: 39,379,684-39,509,376 , GRCh37.p13 chr8: 39,260,527-39,390,219 , GRCh38.p12 chr8: 39,403,008-39,532,700	ADAM3A, ADAM5
nsv900335	copy number variation	1	nstd71	human		NCBI36 chr13: 63,353,166-63,456,879 , GRCh37.p13 chr13: 64,455,165-64,558,878 , GRCh38.p12 chr13: 63,881,032-63,984,745	NFYAP1, LINC00355
nsv900170	copy number variation	13	nstd71	human		NCBI36 chr13: 56,654,503-56,725,158 , GRCh37.p13 chr13: 57,756,502-57,827,157 , GRCh38.p12 chr13: 57,182,368-57,253,023	LOC105370216, MTCO2P3
nsv886217	copy number variation	1	nstd71	human		NCBI36 chr6: 77,471,874-77,547,436 , GRCh37.p13 chr6: 77,415,155-77,490,717 , GRCh38.p12 chr6: 76,705,438-76,781,000	LOC105377861, LOC105377862
nsv879318	copy number variation	371	nstd71	human		NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558	LOC728807, UGT2B17, 2 more genes
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv892329	copy number variation	1	nstd71	human		NCBI36 chr9: 10,676,548-10,813,141 , GRCh37.p13 chr9: 10,686,548-10,823,141 , GRCh38.p12 chr9: 10,686,548-10,823,141	0

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